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RUNNING FOR RYAN

Michael Briggs is raising money for The Society For Mucopolysaccharide Diseases (The MPS Society)

Participants: Ed Challinor

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Flora London Marathon 2007 · 22 April 2007 ·

The MPS Society provides specialist support to children, adults and families in the UK who are affected by MPS, Fabry and related lysosomal storage diseases and we fund research into treatment and therapies. These diseases are rare, genetic, life-limiting conditions with no cure.

Story

Thank you for visiting my fundraising page. Please dig deep and sponsor me online. You will be helping Ryan who has Hunter Disease, a horrible life limiting condition, and needs all the support he can get.  Read the latest news about Ryan and the battle to get treatment on http://home.btconnect.com/Ryans-page/ and click on Lates News.

Thev MPS Society has three main aims:

  1. To act as a support network for those affected by MPS and related diseases.
  2. To bring about more public awareness of MPS and related diseases.
  3. To promote and support research into MPS and related diseases.


Donating through this site is simple, fast and totally secure. It is also the most efficient way to sponsor me: The Society For Mucopolysaccharide Diseases will receive your money faster and, if you are a UK taxpayer, an extra 28% in tax will be added to your gift at no cost to you.

So, even though I finished the Marathon (dressed as a Centurion, as you can see on the photo of me with girlfriend Anna) please still sponsor me now!

Many thanks for your support.

Donation summary

Total
£10,038.50
+ £838.26 Gift Aid
Online
£5,713.50
Offline
£4,325.00

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